hello my friends, after having had body tremors and shaking hand since I was a small boy, I had an appointment with a Neurologist at my local hospital on Saturday 3rd February, and he sent a letter to my GP, and a copy to me, stating that I had Ataxia, but he didn’t say which type.
I have used an electric wheelchair to get about outside for nigh on twenty years, can’t walk in a straight line, but get tired and exhausted anyway…… I use furniture, walls and doorframes to walk around indoors…… my county council(Kent) put a disabled parking bay outside my house, and lowered the curb, my local council converted my bathroom inti a wetroom, with shower and safety bars, and also installed a through the floor lift from my dining room up to the small bedroom…… all this at no expence to me
Hoping you can all get out to enjoy the forthcoming spring/summer.
Take care and stay safe out there folks.
Don(Veteran250)
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Veteran250
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Sorry to hear of all your problems. I hope now the council have installed aids for you that life will be that much better for you. Thank goodness we have the summer to look forward to. It has been a long miserable winter with all the rain, so hope you will be able to get out and about very soon. We all need a break l think. Keep smiling through and keep safe.
Good to hear from you Veteran250. It sounds as if your local council is unusually caring. I have body tremors now and put it down to Pregabalin but I'm not sure. I've been asleep all day pretty much and think I overdosed last night. Or just tiired. I will go to bed soon.
Hi Don. Its great that you've been able to have your house adapted in so many ways. Must be of great benefit to you. Like all the others on here am looking forward to being able to get outside in the garden
Hello Don, firstly I hope you are the best you can be it’s unbelievably difficult suffering with ataxia no matter what type.
I’m so pleased your local authorities have recognised your needs and provided you with the essentials to get by every day.
My local council and city council have done the same for me although I had to pay a contribution towards some of the work which wasn’t an issue as it was only a small amount. The wet room and raised toilet is a revelation. Stairs are my nemesis my wife assists me going up and I come down on my bum I have slid down them quite a few times taking skin of my face I’m to big for a stair lift 6’2 15stone 🤨 I have started process with local enablement team for a lift like yours so fingers crossed
hi Don it’s good to hear that you are getting the help that you need.
Yes, I have grab rails wherever I can have them. I really wish it was more easy for me to get outside on my buggy as it has to be stored in the garage.
I don’t often post here because of my infernal, shaking due to neuropathy, however, I am using dictation on this occasion.
I hope we will all be able to get outside soon in that sun and get some real good vitamins. I wish you the very best health and it was lovely to hear from you again.
Hi, I'm glad that your council seem to be doing things to make your life easier. My daughter replies to my messages because it takes me ages to write them. I can't wait for some outside fun. in the sun. All the best x
Hello my lovely, it’s nice to get your message, I don’t visit HU very often either….. I was very surprised to learn that I have had Ataxia all of my life, my hands have shaken ever since I was a small boy, but the Neurologist didn’t elaborate on which type of Ataxia I had….. but life goes on, and I’ve turned 80 now.
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Ataxia sca3 
Genetic Ataxia
